45 results
·
34ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
×
Implant, Corneal, Refractive
FDA Pre-Market Approval
FDA Class 3
·INTACS PRESCRIPTION INSERTS
Implant, Corneal, Refractive
FDA Pre-Market Approval
FDA Class 3
·INTACS PRESCRIPTION INSERTS
Implant, Corneal, Refractive
FDA Pre-Market Approval
FDA Class 3
·INTACS® Corneal Implants
Implant, Corneal, Refractive
FDA Pre-Market Approval
FDA Class 3
·INTACS PRESCRIPTION INSERTS/INTACS CORNEAL IMPLANTS
Implant, Corneal, Refractive
FDA Pre-Market Approval
FDA Class 3
·INTACS PRESCRIPTION INSERTS
Implant, Corneal, Refractive
FDA Pre-Market Approval
FDA Class 3
·INTACS CORNEAL RING SEGMENTS
Implant, Corneal, Refractive
FDA Pre-Market Approval
FDA Class 3
·INTACS PRESCRIPTION INSERTS
Implant, Corneal, Refractive
FDA Pre-Market Approval
FDA Class 3
·INTACS PRESCRIPTION INSERTS
Implant, Corneal, Refractive
FDA Pre-Market Approval
FDA Class 3
·INTACS (INTRASTROMAL CORNEAL RING SEGMENTS)
Implant, Corneal, Refractive
FDA Pre-Market Approval
FDA Class 3
·INTACS PRESCRIPTION INSERTS/INTACS CORNEAL IMPLANTS
Implant, Corneal, Refractive
FDA Pre-Market Approval
FDA Class 3
·INTACS PRESCRIPTION INSERTS
Implant, Corneal, Refractive
FDA Pre-Market Approval
FDA Class 3
·INTACS CORNEAL IMPLANTS
Implant, Corneal, Refractive
FDA Pre-Market Approval
FDA Class 3
·INTACS (INTRASTROMAL CORNEAL RING SEGMENTS)
Implant, Corneal, Refractive
FDA Pre-Market Approval
FDA Class 3
·INTACS CORNEAL IMPLANTS
Sensor, Glucose, Invasive
FDA Pre-Market Approval
FDA Class 3
·DEXCOM SEVEN & SEVEN PLUS SYSTEM
Heart-Valve, Non-Allograft Tissue
FDA Pre-Market Approval
FDA Class 3
·TRIFECTA VALVE WITH GLIDE TECHNOLOGY
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·Astra XT DR MRI IPG, Astra S DR MRI IPG, Astra S SR MRI IPG, Astra XT SR MRI IPG, Azure S DR MRI IPG, Azure S SR MIR IPG
Catheter, Coronary, Atherectomy
FDA Pre-Market Approval
FDA Class 3
·ROTABLATOR ROTATIONAL ANGIOPLASTY SYSTEM GUIDE WIRES
Intracranial Aneurysm Flow Diverter
FDA Pre-Market Approval
FDA Class 3
·Pipeline Flex Embolization Device, Pipeline Flex Embolization Device with Shield Technology
Agent, Bulking, Injectable For Gastro-Urology Use
FDA Pre-Market Approval
FDA Class 3
·DURASPHERE INJECTABLE BULKING AGENT